Canonical Allele Identifier: PA2828000214
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg323His
CA004108
NM_001354902.2:c.968G>A